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Bioprinting of Hydrogel Tumor Slices as a 3D Model for Mantle Cell Lymphoma
Published on: September 12, 2025
Novel agents in mantle cell lymphoma
Marcus S Noel1, Jonathan W Friedberg, Paul M Barr
1University of Rochester Medical Center, James P. Wilmot Cancer Center, 601 Elmwood Avenue, Box 704, Rochester, NY 14642, USA. marcus_noel@urmc.rochester.edu
Novel agents show promise for treating mantle cell lymphoma (MCL), a rare non-Hodgkin lymphoma with a poor prognosis. Early trials highlight targeted therapies and BH-3 mimetics for improved patient outcomes.
Area of Science:
- Oncology
- Hematology
- Molecular Biology
Background:
- Mantle cell lymphoma (MCL) is a mature B cell neoplasm comprising 5-7% of non-Hodgkin lymphomas.
- Current therapeutic options for MCL offer a poor overall prognosis, necessitating the development of novel treatments.
Purpose of the Study:
- This review focuses on early-phase clinical trials investigating promising novel agents for mantle cell lymphoma.
- To highlight the potential of targeted signaling pathway inhibition and other emerging therapies in MCL treatment.
Main Methods:
- Review of early-phase clinical trials in mantle cell lymphoma.
- Analysis of targeted agents including inhibitors of spleen tyrosine kinase, phosphoinositide 3-kinase, and Bruton's tyrosine kinase.
- Evaluation of BH-3 mimetics and histone deacetylase inhibitors in MCL.
Main Results:
- Early trials demonstrate promise for novel agents targeting key signaling pathways in MCL.
- Inhibitors of spleen tyrosine kinase, phosphoinositide 3-kinase, and Bruton's tyrosine kinase are under active investigation.
- BH-3 mimetics and histone deacetylase inhibitors also show potential in MCL treatment.
Conclusions:
- Targeting B cell receptor signaling pathways offers a promising therapeutic strategy for mantle cell lymphoma.
- Further understanding of cellular signaling will expand treatment options and improve MCL prognosis.
- Novel agents in early-phase trials hold hope for enhancing the therapeutic armamentarium against MCL.
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